Ccbe1 Mutations Can Cause A Mild, Atypical Form of Generalized Lymphatic Dysplasia but Are Not A Common Cause of Non-Immune Hydrops Fetalis

Clinical GeneticsVolume 81, Issue 2 p. 191-197 CCBE1 mutations can cause a mild, atypical form of generalized lymphatic dysplasia but are not a common cause of non-immune hydrops fetalis FC Connell, FC Connell Clinical Genetics Department, Guy's and St Thomas' NHS Foundation Trust, London, UK Both these authors contributed equally to this work.Search for more papers by this authorK Kalidas, K Kalidas Medical Genetics Both these authors contributed equally to this work.Search for more papers by this authorP Ostergaard, P Ostergaard Medical GeneticsSearch for more papers by this authorG Brice, G Brice Southwest Thames Regional Genetics Service, St. George's University of London, UKSearch for more papers by this authorV Murday, V Murday Ferguson-Smith Centre for Clinical Genetics, Yorkhill Hospital, Glasgow, UKSearch for more papers by this authorPS Mortimer, PS Mortimer Department of Cardiac and Vascular Sciences (Dermatology)Search for more papers by this authorI Jeffrey, I Jeffrey Perinatal Pathology, St George's University of London, London, UKSearch for more papers by this authorS Jeffery, S Jeffery Medical GeneticsSearch for more papers by this authorSahar Mansour, Corresponding Author Sahar Mansour Southwest Thames Regional Genetics Service, St. George's University of London, UKSahar MansourSouthwest Thames Regional Genetics ServiceSt. George's University of LondonLondon SW17 0RE UKTel.: +44 2087250957Fax: +44 2087253444e-mail: smansour@sgul.ac.ukSearch for more papers by this author FC Connell, FC Connell Clinical Genetics Department, Guy's and St Thomas' NHS Foundation Trust, London, UK Both these authors contributed equally to this work.Search for more papers by this authorK Kalidas, K Kalidas Medical Genetics Both these authors contributed equally to this work.Search for more papers by this authorP Ostergaard, P Ostergaard Medical GeneticsSearch for more papers by this authorG Brice, G Brice Southwest Thames Regional Genetics Service, St. George's University of London, UKSearch for more papers by this authorV Murday, V Murday Ferguson-Smith Centre for Clinical Genetics, Yorkhill Hospital, Glasgow, UKSearch for more papers by this authorPS Mortimer, PS Mortimer Department of Cardiac and Vascular Sciences (Dermatology)Search for more papers by this authorI Jeffrey, I Jeffrey Perinatal Pathology, St George's University of London, London, UKSearch for more papers by this authorS Jeffery, S Jeffery Medical GeneticsSearch for more papers by this authorSahar Mansour, Corresponding Author Sahar Mansour Southwest Thames Regional Genetics Service, St. George's University of London, UKSahar MansourSouthwest Thames Regional Genetics ServiceSt. George's University of LondonLondon SW17 0RE UKTel.: +44 2087250957Fax: +44 2087253444e-mail: smansour@sgul.ac.ukSearch for more papers by this author First published: 12 January 2012 https://doi.org/10.1111/j.1399-0004.2011.01731.xCitations: 20 Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat Citing Literature Volume81, Issue2February 2012Pages 191-197 RelatedInformation